| Tag | Content |
|---|
EnhancerAtlas ID | HS092-19904 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr16:88838310-88841280 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr16:88840520-88840534 | GGGTGGGCGTGGCC | - | 6.69 | | Klf12 | MA0742.1 | chr16:88840519-88840534 | TGGGTGGGCGTGGCC | - | 6.28 | | Nr2f6(var.2) | MA0728.1 | chr16:88838970-88838985 | GAGGTCAACAGATCA | + | 6.15 | | Nr5a2 | MA0505.1 | chr16:88839947-88839962 | GGGCTCAAGGCCACC | + | 6.07 | | PLAG1 | MA0163.1 | chr16:88839594-88839608 | CCCCCTCTGGCCCC | - | 6.18 | | SP1 | MA0079.4 | chr16:88840521-88840536 | GGTGGGCGTGGCCTG | - | 7.44 | | SP3 | MA0746.2 | chr16:88840521-88840534 | GGTGGGCGTGGCC | - | 7.52 | | SP4 | MA0685.1 | chr16:88840519-88840536 | TGGGTGGGCGTGGCCTG | - | 7.05 | | SP8 | MA0747.1 | chr16:88840521-88840533 | GGTGGGCGTGGC | - | 6.62 | | ZNF263 | MA0528.1 | chr16:88839763-88839784 | GGAGGAGGTGGGCAGGGGGAG | + | 6.08 |
|
| | Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
| SE_19495 | chr16:88839529-88840681 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20944 | chr16:88833062-88841844 | CD8_Memory_7pool | | SE_26909 | chr16:88838435-88840646 | Esophagus | | SE_26909 | chr16:88840699-88841897 | Esophagus | | SE_41570 | chr16:88838421-88839005 | LNCaP | | SE_41570 | chr16:88839199-88841823 | LNCaP | | SE_42993 | chr16:88839041-88841790 | Lung | | SE_45418 | chr16:88838420-88841550 | NHLF | | SE_47797 | chr16:88838526-88839006 | Pancreas | | SE_47797 | chr16:88839163-88840165 | Pancreas | | SE_50742 | chr16:88839023-88841254 | Sigmoid_Colon | | SE_53797 | chr16:88839090-88840673 | Spleen | | SE_54707 | chr16:88832832-88841883 | Stomach_Smooth_Muscle | | SE_56985 | chr16:88838441-88838803 | VACO_400 | | SE_56985 | chr16:88839162-88839582 | VACO_400 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I088766 | chr16 | 88833274 | 88841799 |
|
Enhancer Sequence | TCCTGAGACT CTATGCCCGT CCACCCGCGG CCCCAGGCCC ACCTGAGACT CTATGCCCGT 60
CCACCCGCGG CCCCAGGCCC TCCTGAGACT CTATGCCCAT CCACCCGCGG CCCCAGGCCC 120
TCCTGAGACT CTATGCCCGT CCACCCGCGG CCCCAGGCCC ACCTGAGACT CTATGCCTGT 180
CCACCCGCGG CCCCAGGCCC TCCTGAGACT CTGGTCAGGA TGCCTGTCCA CCTGCGGCCC 240
CAGGCCCTCC TGAGACTCTG GGCATGGCTG TCAGAATGAC CATCCCTGGT GCCATTGAGA 300
CCCCAGATCC AGCACCTGTG TCCAGCGCTG AAGTCCCAAG TCTGTGTCCA AGCTCAGAAG 360
GAGGGCCCAG AATCCCAGAC GTATCATGGC AGCAAGTGAG CCGGGGGTTG GGACAGGTAA 420
GCAGGCTCTT GTGGCTTAGC CACCAGCTCG GAATATACTT TCCATGTGGA CATGAGGCCC 480
AGGTGCCAAT AACCAACAGC CACGCTGGAG CTGAGGGCCC TGGGAGCCTG CAGGCCCCAG 540
CCCACAGGCA GGTGGCAGAG GGCACGGCTT CCTCCCTCAT AAAAAGGCCC GTGCCTGGCA 600
GGGCACAGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGCA AGCAGATCAC 660
GAGGTCAACA GATCAAGACC ATCCTGGACA ACATGGTAAA ACCCCGTCTC TACTAAAAAT 720
ACAAAAATGA GCCGGGCGTG ATGGTGGGTG CCTGTAATCT CAGCTACTGG GGAGGCTGAG 780
GCAGGAGAAT CGCTTGAACC TGGGAGGCGA AGGTGGCAGT GAGCTGAGAT CGTGCCACTG 840
CATTCCAGCC TGGCCAAAGA GTGAGACTCT GTCAAAAAAA AAAAAAAAAA GGCCTGTGCC 900
CCCTCCTCCC TGTTCTCTGA GGGGGATGCC CGCCGCAGCC CTGGCTCAGT CTTCATGTCA 960
CCCCCTTGCA AATGTGCAAG CTCCTGAGGC CGCAGGCTGG GGTGGGCCAT GGCAGGGCCA 1020
GCCTCCCCTC CAAACACCCA CGGGACACGT GAGTGGAGGC ACATGGCTTC CAGCTGGCCC 1080
CAGGGGTGCC TGGAAGACTG TGTCAGCCTC TGGAATGTGA GGCGGCCTGT CTGTCCACCC 1140
AGAAGCTTCT GGCACTCCAG GGAGCTCGAG CTCGCTGTGC TCTGGAAGCA GCAATTACTC 1200
CTCCATCTGT CACCAGCGGC TCCAGCCAGC CCTCAGGTCC ACGTGCCTCC TTCCTCCTGG 1260
GTCTCATTGA TTCAGGCTGA GCCTCCCCCT CTGGCCCCCC AGTAACTCCC GGCGTCACGC 1320
CCAGGCCCTC GCTCAGGGGA TCTGAGTAGA GGGGAGGCCT GAGTCAGGAC AGCCCTCCAA 1380
GAGTGGGCAG CCAACGAGGG ACCCCCTGAA TAAAAACCGC AGAGGAGGTC TGCCCACCTG 1440
GCGTGGGGGC CAGGGAGGAG GTGGGCAGGG GGAGGGGCCT TGCCCGAGAC CAGAGGTGGC 1500
TGGGGGCCGA GGGTCGGCAG GAAGCCAGGC GACCGATGGG CGCAGCACAG ACTGCCTCCA 1560
CGTGGCCCTG CACAGCCTGG CCTCACTAGG GGAAGGGTGA AGACAGCAGC TGGCGCTTCC 1620
CCTCAAAAAA ACCCTGGGGG CTCAAGGCCA CCCCTGAGGT CTCCAGGCTC CTAGGAACAG 1680
GGCCTGACAG GGAAAAGGCT GACAGGCAGG TCGGGGGACT GGACAGCAGC TGCCTATTGG 1740
GTGACAGGCA GGTCGGGGGA GTGGACAGCA GCTGCCTACT GGGTGACAGG CAGGTCGGGG 1800
GAGTGGACAG CAGCTGCCTA CTGGGTGACA GGCAGGTCGG CGGAGTGGAC AGCAGCTGCC 1860
TACTGGGGGT GAGGGCTCCG GCCACCCTGC ACCCAGTGTC CTCCTGGGTG GTCTTAGGAA 1920
GAGGGTCACT CGACCCCAGC CCTCCAGTGC AGGGCCCCAC CGGAGCTTGC TCTGGGCACT 1980
TCTGGCCCTG CCAAAAGTCC CCTCAGGTGC CACCATCCCT GACCACCAAC ACCTCCCTGC 2040
AGGTCCCCCG AGTCCCTTCA GCACCGCAAG CCTCCTCCCC GCCACTGCTG ACCTTCAGAG 2100
ATTGGGGCCC CTCCAGGCCT CCCTCTCCCC TGGCTTGGAA GTTCTGTGCC CGGCGATAAG 2160
GTCTGGGATG CAGCTCCCAA CACAGCAGGA ACCGGTCACC AGGCAGGGCT GGGTGGGCGT 2220
GGCCTGAGCT TCTAAGCGCA TGACTGTCAC CTCCTCCTGG CCTCTGCCTG GGCCCCCTTC 2280
CCACCCACAG GATGGCGACG CCCAGTGACT CCCTGACCAG GCTGTAATAA TATAAACTAG 2340
AGGTCCAGCC TGGTGATACA TGCCTGTAAT CCCAGCTACT CAGGAGGCTG AGGCATGAGA 2400
ATCGCTTGAA CCCGGGAGGC GGAGTTTGCG ATGAGTCGAG ATTGTGCCAC TGCACACCAG 2460
CTTGGGCGAC AGAGCGAGAC TCTGTCTCGA TAAGTAAATA AATAAAAATA ACAATATAAA 2520
CTGGAGAAAG ACACCCGTGG GTGCTGAAGG GGAAAACAGG ACCCAGCTGT GATAGCCAGG 2580
ACAGCTCAGG GTCAAGGAGA CTCACTCCTG GGCTCCAGAG TCCCCAGCAG CAGCCTGGGC 2640
ACCTCTGTAT ACCACGTGGA GGAGAAACGG GTGGGCATCG CTGGCCCAGC TGCAGGTCTG 2700
AGTGGGGGTC CCAGGAAGCC TGAAAAGGAA GCCGGCAATC CCGCGCTGGA CCCATGAAGA 2760
AGGGCCGACC AGACAAGGAT GGGGCCCAAG GGCAAAGAGA CCGCTTGTCT TATGCCACAG 2820
TGGCTGGGGA GAGCACTCTT AGGGTACATG GGGTTCCCTG CAGGATTCCG CAAAAACAGG 2880
GCACCCCGGA GCCGGCTGCG CAGGAGCGAA CGGTGCCCAC ATGGTCTAAG ATACCTCAGC 2940
ACAGCCTCCT GGGCGCTGAA ACCACCCAGG 2970
|
